Evidence mapPaperPMID 35192550Full record

Trial reportJCI insight2022

Acute aerobic exercise reveals that FAHFAs distinguish the metabolomes of overweight and normal-weight runners.

Alisa B Nelson, Lisa S Chow, David B Stagg, Jacob R Gillingham, Michael D Evans, Meixia Pan, Curtis C Hughey, Chad L Myers, Xianlin Han, Peter A Crawford and 1 more

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in JCI insight, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02150889 (Training Effects on Fuel Metabolism), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02150889 naactive not recruitingnot on this map

Training Effects on Fuel Metabolism

TypeinterventionalSponsorUniversity of MinnesotaRan2014 to 2026Enrolled64ConditionsHealthy Subjects, Lean Trained Subjects, Overweight and ObesityArmsRunning Program, Yoga Program
3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. PAHSAs reduce cellular senescence and protect pancreatic beta cells from metabolic stress through regulation of Mdm2/p53.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Alisa B NelsonDivision of Molecular Medicine, Department of Medicine.
Lisa S ChowDivision of Diabetes, Endocrinology and Metabolism, Department of Medicine.
David B StaggDivision of Molecular Medicine, Department of Medicine.
Jacob R GillinghamDivision of Molecular Medicine, Department of Medicine.
Michael D EvansBiostatistical Design and Analysis Center, Clinical and Translational Science Institute, University of Minnesota, Minneapolis, Minnesota, USA.
Meixia PanBarshop Institute for Longevity and Aging Studies and.
Curtis C HugheyDivision of Molecular Medicine, Department of Medicine.
Chad L MyersBioinformatics and Computational Biology Program.
Xianlin HanBarshop Institute for Longevity and Aging Studies and.
Peter A CrawfordDivision of Molecular Medicine, Department of Medicine.
Patrycja PuchalskaDivision of Molecular Medicine, Department of Medicine.

Funding

NCATS NIH HHS UL1 TR000114NCATS NIH HHS UL1 TR002494NIA NIH HHS R01 AG069781NIDDK NIH HHS R01 DK091538NIDDK NIH HHS R01 DK098203
6 · The paper itself

Abstract

BackgroundResponses of the metabolome to acute aerobic exercise may predict maximum oxygen consumption (VO2max) and longer-term outcomes, including the development of diabetes and its complications.MethodsSerum samples were collected from overweight/obese trained (OWT) and normal-weight trained (NWT) runners prior to and immediately after a supervised 90-minute treadmill run at 60% VO2max (NWT = 14, OWT = 11) in a cross-sectional study. We applied a liquid chromatography high-resolution-mass spectrometry-based untargeted metabolomics platform to evaluate the effect of acute aerobic exercise on the serum metabolome.ResultsNWT and OWT metabolic profiles shared increased circulating acylcarnitines and free fatty acids (FFAs) with exercise, while intermediates of adenine metabolism, inosine, and hypoxanthine were strongly correlated with body fat percentage and VO2max. Untargeted metabolomics-guided follow-up quantitative lipidomic analysis revealed that baseline levels of fatty acid esters of hydroxy fatty acids (FAHFAs) were generally diminished in the OWT group. FAHFAs negatively correlated with visceral fat mass and HOMA-IR. Strikingly, a 4-fold decrease in FAHFAs was provoked by acute aerobic running in NWT participants, an effect that negatively correlated with circulating IL-6; these effects were not observed in the OWT group. Machine learning models based on a preexercise metabolite profile that included FAHFAs, FFAs, and adenine intermediates predicted VO2max.ConclusionThese findings in overweight human participants and healthy controls indicate that exercise-provoked changes in FAHFAs distinguish normal-weight from overweight participants and could predict VO2max. These results support the notion that FAHFAs could modulate the inflammatory response, fuel utilization, and insulin resistance.Trial registrationClinicalTrials.gov, NCT02150889.FundingNIH DK091538, AG069781, DK098203, TR000114, UL1TR002494.

Indexed as

EstersOverweightAdenineCross-Sectional StudiesExerciseFatty AcidsHumansMetabolomeObesityAdenineEstersFatty AcidsAdipose tissueDiabetesMetabolismObesity

Identifiers

PMID35192550
PMCPMC9057596

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.